NCT04246970Enrolling by invitation
Prehabilitation and Posttransplant Training Program in Liver Transplantation
Effects of a Prehabilitation Program in Liver Transplant Candidates Followed by a Posttransplant Training Program
Source: ClinicalTrials.gov · Last updated 15 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
PreLiveR-T consists of a prospective randomized clinical trial conducted in an adult population that is a candidate for liver transplantation (LT) at the Hospital La Fe Valencia (Spain). The study is structured in three phases: I) Prehabilitation (2 months before LT); II) Training, divided in two successive periods: Supervised training (months 3-6 after LT) and Unsupervised training (6-12 months after LT); III) Long-term follow-up (2 years after LT). Primary outcomes are related to post-surgery evolution (morbidity and mortality, hospitalization length, etc.). As a secondary outcomes are collected those related to: functional capacity, muscle strength and quality of life.
- Status (registry)
- Enrolling by invitation
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- First submitted
- 20 Jan 2020
- Start date
- 1 Apr 2021
- Primary completion date
- Jun 2026
- Lead sponsor
- Maria dels Angels Cebria i Iranzo, PT, PhD
- Diseases
- Liver and biliary tract cancer
- NCT number
- NCT04246970
What you commit to
- Study type: Interventional
- Planned participants: 60
- From 1 Apr 2021 to the primary completion date, Jun 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Esophageal varices not treated with ligature or beta-blockers
- Multi-organ transplantation and liver retransplantation
Other illness
- Varicose veins with a high risk of digestive hemorrhage
Lab values
- Hemoglobin \<80 g/l
Other
- Any orthopedic, motor, functional, neurological, cognitive or linguistic limitation that prevents the realization of the Prehabilitation program
- Inability to perform psychometric tests
- Contraindication to weight loading
- Impossibility to comply with the Prehabilitation program (hospital admission, work, geographical location)
- Refusal or lacks capacity to give informed consent
Who the study is looking for
- Indication of elective liver transplant with favorable cardiorespiratory evaluation that does not contraindicate the transplant.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hospital Universitari i Politécnic La Fe Coordinator of this site? Confirm its status | Valencia | Spain | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.